Senior Clinical Research Associate - Rare CNS - Southeast/Mid-Atlantic (Remote)

Worldwide Clinical Trials; Maryland; Vor Ort; USD 97.000 - 193.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking a Clinical Research Associate in the United States Southeast/Mid-Atlantic region. You will manage research activities at sites participating in multiple therapeutic areas, coordinating regulatory documents, contracts, budgets, and data collection to ensure compliant study execution.

The role involves remote site-management, regular coaching, and a clear career path toward Clinical Trial Manager roles, with strong emphasis on quality and collaboration across

Qualifikationen

• 5+ years of experience as a Clinical Research Associate.
• 4-year university degree or Nursing Degree.
• Experience in Rare CNS is required.
• Candidates must reside in the southeastern or Mid‑Atlantic United States.
• Willingness to travel regionally required.

Aufgaben

• Manage the research activities at sites participating in Worldwide’s clinical research projects.
• Involve in all stages of the clinical study, including site startup, contracts and budgets, site training, and safety reporting.
• Conduct study initiation visits (SIVs).
• Most site-management will be remote, with compliance to consent, safety, and regulatory requirements.

Kenntnisse

Communication

Organizational skills

Independent work

Ausbildung

4-year University Degree

Nursing Degree

Tools

Microsoft Office

CTMS

EDC Systems

Jobbeschreibung

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Clinical Operations Does At Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

As a Clinical Research Associate (CRA) at Worldwide, you will work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top‑tier colleagues from various backgrounds and specialties is not just encouraged; it’s ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team‑oriented environment. In a CRA role, you’ll receive extensive support through regulatory submissions, TMF management, and in‑house CRAs for projects with heavy site‑management needs.

Through regular touchpoints and coaching conversations with your Line Manager, we ensure your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science.

We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!

What You Will Do

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Typically involved in all stages of the clinical study, including identifying potential sites to participate, performing start‑up activities such as working with sites to collect appropriate regulatory documents, supporting the negotiation of contracts and budgets, training sites to collect data properly, reporting any potential safety‑related events, managing the site’s activities during study maintenance, and closing down research activities once the study has concluded
• Conduct study initiation visits (SIVs)
• Most of the site‑management efforts will be performed remotely, but you will be required to ensure compliance with obtaining informed consent, reporting potential safety‑related events, and adhering to all applicable regulatory requirements

What You Will Bring To The Role

• Excellent interpersonal, oral, and written communication skills in English
• Superior organizational skills with attention to detail
• Ability to work with little or no supervision
• Proficiency in Microsoft Office, CTMS, and EDC Systems

Your Experience

• 5+ years of experience as a Clinical Research Associate
• 4‑year university degree or Nursing Degree
• Experience in Rare CNS is required
• Candidates must reside in the southeastern or Mid‑Atlantic United States
• Willingness to travel regionally required

Compensation and Benefits

We are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (for hourly paid positions, the stated salary range reflects hourly rates):

• United States of America – $97,000.00 – $193,000.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it is not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

EEO Statement

We are committed to fostering an inclusive and equitable workplace.